产品说明
包装
5, 25 mg in glass bottle
生化/生理作用
UCM710 is a dual inhibitor of fatty acid amide hydrolase (FAAH) and α/β hydrolase domain 6 (ABHD6) the enzymes that hydrolyze endocannabinoids. UCM710 augments both N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol (2-AG) levels in neurons. UCM710 does not inhibit monoacylglycerol lipase (MAGL).
特点和优势
This compound is featured on the Cannabinoid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
基本信息
经验(实验)分子式 | C19H34O3 |
分子量 | 310.47 |
MDL编号 | MFCD22666406 |
PubChem化学物质编号 | 329825523 |
NACRES | NA.77 |
产品性质
质量水平 | 100 |
测定 | ≥98% (HPLC) |
形式 | oil |
颜色 | colorless to light yellow |
储存温度 | 2-8℃ |
SMILES string | CCCCCC\C=C/CCCCCCCC(=O)OCC1CO1 |
InChI | 1S/C19H34O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(20)22-17-18-16-21-18/h7-8,18H,2-6,9-17H2,1H3/b8-7- |
InChI key | FWEHVPCBXKCYHE-FPLPWBNLSA-N |
安全信息
储存分类代码 | 12 - Non Combustible Liquids |
WGK | WGK 3 |
闪点(F) | Not applicable |
闪点(C) | Not applicable |